US6268489B1 - Azithromycin dihydrate - Google Patents
Azithromycin dihydrate Download PDFInfo
- Publication number
- US6268489B1 US6268489B1 US07/994,040 US99404092A US6268489B1 US 6268489 B1 US6268489 B1 US 6268489B1 US 99404092 A US99404092 A US 99404092A US 6268489 B1 US6268489 B1 US 6268489B1
- Authority
- US
- United States
- Prior art keywords
- azithromycin
- water
- dihydrate
- water content
- monohydrate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- MQTOSJVFKKJCRP-UHFFFAOYSA-N CCC1OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC2OC(C)CC(N(C)C)C2O)C(C)(O)CC(C)CN(C)C(C)C(O)C1(C)O Chemical compound CCC1OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC2OC(C)CC(N(C)C)C2O)C(C)(O)CC(C)CN(C)C(C)C(O)C1(C)O MQTOSJVFKKJCRP-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
- C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
- C07D239/545—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
- C07H17/04—Heterocyclic radicals containing only oxygen as ring hetero atoms
- C07H17/08—Hetero rings containing eight or more ring members, e.g. erythromycins
Definitions
- the present invention is directed to a valuable new form of azithromycin (9-deoxo-9a-aza-9a-methyl-9a-homoerythromycin A), viz., a non-hygroscopic dihydrate form thereof.
- Azithromycin is the U.S.A.N. (generic name) for 9-deoxo-9a-aza-9a-methyl-9a-homoerythromycin A, a broad spectrum antibacterial compound derived from erythromycin A.
- Azithromycin was independently discovered by Bright, U.S. Pat. No. 4,474,768 and Kobrehel et al., U.S. Pat. No. 4,517,359.
- the name “N-methyl-11-aza-10-deoxo-10-dihydroerythromycin A” was employed in these patents. The present more systematic name is based upon the ring expansion and replacement nomenclature of the “IUPAC Nomenclature of Organic Chemistry, 1979 Edition,” Pergamon Press, 1979, pp. 68-70, 459, 500-503.
- azithromycin was obtained as a hygroscopic monohydrate (for details, see Preparation 1 below). Because of its hygroscopic nature, it is most difficult to prepare and maintain this prior monohydrate product in a form having a constant, reproducible water-content. It is particularly difficult to handle during formulation, since at higher relative humidity levels which are generally required to avoid electrostatic problems (e.g., flow rates, dusting with potential for explosion), the monohydrate readily picks up varying amounts of water, the amount depending upon exposure time and the precise value of the relative humidity (see Preparation 1 below). Such problems have been overcome by the present invention of a stable dihydrate which is essentially non-hygroscopic under conditions of relative humidity conducive to formulation of azithromycin.
- the present invention is directed to a valuable new form of azithromycin, viz., a crystalline, non-hygroscopic dihydrate, prepared by crystallization from tetrahydrofuran and an aliphatic (C 5 -C 7 )hydrocarbon in the presence of at least two molar equivalents of water.
- Azithromycin is of the formula
- erythromycin A It is derived from erythromycin A without involvement of asymmetric centers, and so has stereochemistry at each of these centers (*) which is identical with that of erythromycin A.
- the compound Named systematically as an erythromycin A derivative, the compound is called 9-deoxo-9a-aza-9a-methyl-9a-homoerythromycin A.
- Azithromycin including the present dihydrate, possess broad-spectrum antibacterial activity useful in the treatment of susceptible bacterial infections in mammals, including man.
- aliphatic (C 5 -C 7 )hydrocarbon refers to lower boiling hydrocarbon solvents, frequently mixtures of particular boiling point ranges such as those generally referred to as “pentane”, “hexane”, “hexanes”, etc., but which may also be substantially pure, e.g., n-hexane, cyclohexane or methylcyclohexane.
- a preferred hydrocarbon solvent is so-called “hexane”, having a boiling point which ranges near that of pure n-hexane.
- Azithromycin prepared according to Bright or Kobrehel et al. (cited above) in amorphous form, or as the monohydrate (which may contain, because of its hygroscopicity, more than one molar equivalent of water) is dissolved in tetrahydrofuran. Since the temperatures required for the initial stages of the present process are not critical, ambient temperatures are generally employed, avoiding the cost of heating and cooling. Furthermore, to maximize yield and minimize solvent, labor and equipment costs, the volume of tetrahydrofuran is kept to a near minimum, e.g., 2 liters of solvent per kilogram of substrate. Any insoluble impurities which may be present at this stage are readily removed by conventional methods of filtration.
- the mixture can be decolorized with activated carbon.
- the highly concentrated mixture can be diluted with a portion of (C 5 -C 7 )hydrocarbon prior to filtration, in order to facilitate handling.
- a drying agent such as MgSO 4 , particularly if hydrocarbon solvent is to be added prior to filtration.
- water is added to the resulting clear solution, in an amount sufficient to bring the total water content to a level corresponding to at least two molar equivalents, generally not exceeding a level of about 3-4 molar equivalents.
- the level of water present in the system is readily monitored by standard Karl Fischer titration.
- the addition of water is followed by the addition of the hydrocarbon solvent (or of more hydrocarbon solvent, if the mixture was previously diluted before filtration), leading to crystallization of the desired dihydrate product.
- This stage of the process can be carried out at ambient temperature (e.g. 17-30° C.), but to facilitate the initial crystallization, is preferably carried at slightly elevated temperature (e.g. 30-40° C.).
- the total volume of hydrocarbon solvent employed is generally at least about four times in volume that of the tetrahydrofuran. Higher volumes of hydrocarbon are satisfactory, but are generally avoided in the interest of minimizing cost.
- the product is recovered by filtration, usually after a period of granulation (e.g., 3-24 hours) at ambient temperature.
- the product is usually vacuum dried of organic solvents (at 20-40° C., conveniently at ambient temperature).
- the volatiles and water-content are generally monitored during drying, such that the level of tetrahydrofuran and hydrocarbon will generally fall below 0.25% and the water content will be within 0.3% of theory (4.6%).
- Azithromycin dihydrate is formulated and administered in the treatment of susceptible bacterial infections in man according to methods and in amounts previously detailed by Bright, U.S. Pat. No. 4,474,768, cited above and hereby incorporated by reference.
- the mixture was cooled to ambient temperature, diluted with 400 ml H 2 O and adjusted to pH 10.5 with 50% NaOH.
- the aqueous layer was separated and extracted 2 ⁇ 100 ml with fresh CHCl 3 .
- the organic layers were combined, stripped in vacuo to 350 ml, twice diluted with 450 ml of ethanol and restripped to 350 ml, and finally diluted with 1000 ml H 2 O over a 1 hour period, pausing for 15 minutes as a slurry began to develop after the addition of about 250 ml of H 2 O.
- Title product was recovered by filtration and dried in air at 50° C.
- a sample of the monohydrate (having a water content of 3.2%) was maintained at 18% relative humidity for 14 days.
- the sample lost water over the first 24 hours to yield monohydrate having the theoretical water content (2.35%).
- the water content then remained substantially constant over 14 days, a value of 2.26% being recorded at 14 days.
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cardiology (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Heart & Thoracic Surgery (AREA)
- Biotechnology (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Saccharide Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/994,040 US6268489B1 (en) | 1987-07-09 | 1992-12-21 | Azithromycin dihydrate |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/US1987/001612 WO1989000576A1 (en) | 1987-07-09 | 1987-07-09 | Azithromycin dihydrate |
WOPCT/US87/01612 | 1987-07-09 | ||
US44996189A | 1989-12-11 | 1989-12-11 | |
US07/994,040 US6268489B1 (en) | 1987-07-09 | 1992-12-21 | Azithromycin dihydrate |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US44996189A Continuation | 1987-07-09 | 1989-12-11 |
Publications (1)
Publication Number | Publication Date |
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US6268489B1 true US6268489B1 (en) | 2001-07-31 |
Family
ID=22202456
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US07/994,040 Expired - Lifetime US6268489B1 (en) | 1987-07-09 | 1992-12-21 | Azithromycin dihydrate |
Country Status (45)
Cited By (39)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6528492B1 (en) | 2000-07-25 | 2003-03-04 | Instituto De Investigacion En Quimica Aplicada S.C. | Single-step process for preparing 7, 16-deoxy-2-aza-10-0-cladinosil-12-0-desosaminil-4, 5-dihydroxy-6-ethyl-3,5,9,11,13,15-hexamethylbicycle (11.2.1) hexadeca-1(2)-en-ona and obtaining a new form of 9-deoxo-9a-methyl-9a-aza-9a-homoerythromycin a |
US6583274B1 (en) * | 1999-05-18 | 2003-06-24 | Pfizer Inc. | Crystalline forms of macrolide antibiotic |
US20030162730A1 (en) * | 2001-05-22 | 2003-08-28 | Li Zheng J. | Crystal forms of azithromycin |
US20030165563A1 (en) * | 2001-12-21 | 2003-09-04 | Pfizer Inc. | Directly compressible formulations of azithromycin |
WO2003077830A2 (en) * | 2002-03-18 | 2003-09-25 | Pliva - Istrazivacki Institut D.O.O. | 9-dexo-9a-aza-9a-methyl-9a-homoerythromycin a derivatives |
US20030190365A1 (en) * | 2001-12-21 | 2003-10-09 | Pfizer Inc. | Methods for wet granulating azithromycin |
US20030228357A1 (en) * | 2002-02-01 | 2003-12-11 | Pfizer Inc. | Dry granulated formulations of azithromycin |
US20040023898A1 (en) * | 2001-08-21 | 2004-02-05 | Dunne Michael William | Single dose azithromycin |
US6703372B1 (en) * | 1999-06-29 | 2004-03-09 | Biochemie S.A. | Macrolides |
US20040053862A1 (en) * | 2000-11-27 | 2004-03-18 | Victor Centellas | Macrolide solvates |
US20040092460A1 (en) * | 2002-07-22 | 2004-05-13 | Pliva Pharmaceutical Industry, Incorporated | Novel amorphous 9-deoxo-9a-aza-9a-methyl-9a-homoerythromycin A, process for preparing the same, and uses thereof |
US20040121966A1 (en) * | 2001-05-22 | 2004-06-24 | Pfizer Inc. | Stable non-dihydrate azithromycin oral suspensions |
US20050013835A1 (en) * | 2003-07-15 | 2005-01-20 | Pfizer Inc. | Stable non-dihydrate azithromycin oral suspensions |
US20050123627A1 (en) * | 2003-12-04 | 2005-06-09 | Pfizer Inc | Azithromycin dosage forms with reduced side effects |
US20050123616A1 (en) * | 2003-12-04 | 2005-06-09 | Pfizer Inc | Azithromycin multiparticulate dosage forms by liquid-based processes |
US20050152982A1 (en) * | 2003-12-04 | 2005-07-14 | Pfizer Inc | Controlled release multiparticulates formed with dissolution enhancers |
US20050158391A1 (en) * | 2003-12-04 | 2005-07-21 | Pfizer Inc | Azithromycin multiparticulate dosage forms by melt-congeal processes |
US20050181060A1 (en) * | 2003-12-04 | 2005-08-18 | Pfizer Inc | Method of making pharmaceutical multiparticulates |
US20050181061A1 (en) * | 2003-12-04 | 2005-08-18 | Pfizer Inc | Extrusion process for forming chemically stable drug multiparticulates |
US20050186285A1 (en) * | 2003-12-04 | 2005-08-25 | Pfizer Inc | Multiparticulate compositions with improved stability |
US20050209172A1 (en) * | 2004-03-17 | 2005-09-22 | American Pharmaceutical Partners, Inc. | Lyophilized azithromycin formulation |
US20050222052A1 (en) * | 2002-06-04 | 2005-10-06 | Stefano Turchetta | Process for preparing high purity azithromycin |
US20060063725A1 (en) * | 2004-08-30 | 2006-03-23 | Daniella Gutman | Process of preparing a crystalline azithromycin monohydrate |
US20060116336A1 (en) * | 2004-03-17 | 2006-06-01 | American Pharmaceutical Partners, Inc. | Lyophilized azithromycin formulation |
US20060135548A1 (en) * | 2004-12-01 | 2006-06-22 | Vilmos Keri | Processes for producing crystalline macrolides |
USRE39149E1 (en) | 1994-04-29 | 2006-06-27 | Pfizer Inc. | Method of administering azithromycin |
US20070281894A1 (en) * | 2006-06-05 | 2007-12-06 | Auspex Pharmaceuticals, Inc. | Preparation and utility of substituted erythromycin analogs |
WO2008042139A2 (en) | 2006-10-03 | 2008-04-10 | Dow Pharmaceutical Sciences | Azithromycin for the treatment of nodular acne |
US7414114B2 (en) | 2000-08-23 | 2008-08-19 | Wockhardt Limited | Process for preparation of anhydrous azithromycin |
US20080199527A1 (en) * | 2004-12-21 | 2008-08-21 | Pfizer Inc. | Enteric Coated Azithromycin Multiparticulates |
US20090062220A1 (en) * | 2007-08-29 | 2009-03-05 | Protia, Llc | Deuterium-enriched azithromycin |
WO2010103119A1 (en) | 2009-03-13 | 2010-09-16 | Da Volterra | Compositions and methods for elimination of gram-negative bacteria |
US7887844B2 (en) | 2003-12-04 | 2011-02-15 | Pfizer Inc. | Multiparticulate crystalline drug compositions having controlled release profiles |
US20110184158A1 (en) * | 2008-07-10 | 2011-07-28 | Li Liu | Hydrates of erythromycin salts, preparation and use thereof |
WO2013088274A1 (en) | 2011-12-14 | 2013-06-20 | Wockhardt Limited | Anhydrous amorphous azithromycin composition free of azithromycin dihydrate |
US9326936B2 (en) | 2008-10-07 | 2016-05-03 | Raptor Pharmaceuticals, Inc. | Aerosol fluoroquinolone formulations for improved pharmacokinetics |
US9700564B2 (en) | 2009-09-04 | 2017-07-11 | Horizon Orphan Llc | Use of aerosolized levofloxacin for treating cystic fibrosis |
US10987357B2 (en) | 2005-05-18 | 2021-04-27 | Horizon Orphan, LLC | Aerosolized fluoroquinolones and uses thereof |
US11020481B2 (en) | 2008-10-07 | 2021-06-01 | Horizon Orphan Llc | Topical use of levofloxacin for reducing lung inflammation |
Families Citing this family (37)
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US5912331A (en) * | 1991-03-15 | 1999-06-15 | Merck & Co., Inc. | Process for the preparation of 9-deoxo-9(Z)-hydroxyiminoerythromycin A |
US5985844A (en) * | 1992-03-26 | 1999-11-16 | Merck & Co., Inc. | Homoerythromycin A derivatives modified at the 4"-and 8A-positions |
US5189159A (en) * | 1992-04-02 | 1993-02-23 | Merck & Co., Inc. | 8a-AZA-8a-homoerythromycin cyclic iminoethers |
CA2081268A1 (en) * | 1991-10-25 | 1993-04-26 | Katsuhiro Imaki | Glycine derivative monosodium salt tetrahydrate |
US5215980A (en) * | 1992-01-17 | 1993-06-01 | Merck & Co., Inc. | 10-AZA-9-deoxo-11-deoxy-erythromycin A and derivatives thereof |
US5210235A (en) * | 1992-08-26 | 1993-05-11 | Merck & Co., Inc. | Methods of elaborating erythromycin fragments into amine-containing fragments of azalide antibiotics |
US5332807A (en) * | 1993-04-14 | 1994-07-26 | Merck & Co., Inc. | Process of producing 8A- and 9A-azalide antibiotics |
CN1034734C (zh) * | 1993-12-10 | 1997-04-30 | 北京市集才药物研究所 | 一种新的阿齐红霉素结晶及其制备方法 |
US6068859A (en) | 1994-05-06 | 2000-05-30 | Pfizer Inc. | Controlled-release dosage forms of Azithromycin |
ES2122905B1 (es) * | 1996-07-11 | 1999-11-16 | Astur Pharma Sa | Sintesis de 11,12-hidrogenoortoborato de 9-desoxo-9a-aza-11,12-desoxi-9a-metil-9a-homoeritromicina a. un procedimiento para la preparacion de 9-desoxo-9a-aza-9a-metil-9a-homoeritromicina a dihidrato (azitromicina dihidrato). |
ATE348836T1 (de) * | 1997-10-16 | 2007-01-15 | Glaxosmithkline Zagreb | Neue 3,6-hemiketale der 9a-azalidklasse |
US6861411B1 (en) | 1997-12-02 | 2005-03-01 | Pfizer, Inc. | Method of treating eye infections with azithromycin |
PT102130A (pt) * | 1998-03-13 | 1999-09-30 | Hovione Sociedade Quimica S A | Processo de preparacao de dihidrato de azitromicina |
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DE60133083D1 (de) * | 2000-01-04 | 2008-04-17 | Teva Pharma | Verfahren zur herstellung von azithromycin-dihydrat |
ES2162764B1 (es) * | 2000-05-17 | 2003-04-01 | Ercros Ind Sa | Forma polimorfica del dihidrato de azitromicina, y su procedimiento deobtencion. |
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IN190080B (xx) * | 2001-01-29 | 2003-06-07 | Alembic Ltd | |
KR100491183B1 (ko) | 2001-03-21 | 2005-05-25 | 한미약품 주식회사 | 아지트로마이신의 제조방법 및 이 방법에 사용되는9-데옥소-9에이-아자-9에이-호모에리트로마이신 에이의결정성 수화물 |
EP1652851A1 (en) | 2001-05-22 | 2006-05-03 | Pfizer Products Inc. | New crystal form of Azithromycin |
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US6855813B2 (en) * | 2002-07-19 | 2005-02-15 | Alembic Limited | Process for the preparation of azithromycin monohydrate |
GB2395482A (en) * | 2003-07-03 | 2004-05-26 | Jubilant Organosys Ltd | Process for preparing non-hygroscopic azithromycin dihydrate |
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